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Artigo de periodico-carta/editorial
Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta] (2010)
Brassesco, María Sol; Cortez, Maria Angélica; Valera, Elvis Terci; Engel, Edgard Eduard; Barbosa, Marcello Henrique Nogueira; Becker, Aline Nazareth de Paiva Paixão; Tone, Luiz Gonzaga
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: SARCOMA, CITOGENÉTICA
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ABNT
BRASSESCO, María Sol et al. Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 02 jul. 2025. , 2010
APA
Brassesco, M. S., Cortez, M. A., Valera, E. T., Engel, E. E., Barbosa, M. H. N., Becker, A. N. de P. P., & Tone, L. G. (2010). Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AN de PP, Tone LG. Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta]. Cancer Genetics and Cytogenetics. 2010 ; 197( 1): 86-90.[citado 2025 jul. 02 ]
Vancouver
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AN de PP, Tone LG. Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta]. Cancer Genetics and Cytogenetics. 2010 ; 197( 1): 86-90.[citado 2025 jul. 02 ]
Artigo de periodico
The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival (2010)
Almeida, Luciana Oliveira de; Custódio, Aline Cadurin; Santos, Marcelo José dos; Almeida, José R. W.; Clara, Carlos Afonso; Pinto, Giovanny Rebouças; Rey, Juan A.; Casartelli, Cacilda
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: POLIMORFISMO, NEOPLASIAS CEREBRAIS
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ABNT
ALMEIDA, Luciana Oliveira de et al. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, v. 198, n. 1, p. 15-21, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.11.013. Acesso em: 02 jul. 2025.
APA
Almeida, L. O. de, Custódio, A. C., Santos, M. J. dos, Almeida, J. R. W., Clara, C. A., Pinto, G. R., et al. (2010). The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, 198( 1), 15-21. doi:10.1016/j.cancergencyto.2009.11.013
NLM
Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
Vancouver
Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
Artigo de periodico
Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression (2010)
Brassesco, María Sol; Cortez, Maria Angélica; Valera, Elvis Terci; Engel, Edgard Eduard; Barbosa, Marcello Henrique Nogueira; Becker, Aline Paixão; Scrideli, Carlos Alberto; Tone, Luiz Gonzaga
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: CITOGENÉTICA MOLECULAR, SARCOMA, MULHERES
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ABNT
BRASSESCO, María Sol et al. Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression. Cancer Genetics and Cytogenetics, v. 196, n. 2, p. 189-193, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.10.001. Acesso em: 02 jul. 2025.
APA
Brassesco, M. S., Cortez, M. A., Valera, E. T., Engel, E. E., Barbosa, M. H. N., Becker, A. P., et al. (2010). Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression. Cancer Genetics and Cytogenetics, 196( 2), 189-193. doi:10.1016/j.cancergencyto.2009.10.001
NLM
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AP, Scrideli CA, Tone LG. Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 2): 189-193.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.10.001
Vancouver
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AP, Scrideli CA, Tone LG. Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 2): 189-193.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.10.001
Artigo de periodico
Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas (2010)
Martínez-Glez, Victor; Alvarez, Luis; Franco-Hernández, Carmen; Torres-Martin, Miguel; Campos, Jose M. de; Isla, Alberto; Vaquero, Jesús; Lassaletta, Luis; Castresana, Javier S.; Casartelli, Cacilda; Rey, Juan A.
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: MENINGIOMA, EXPRESSÃO GÊNICA
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ABNT
MARTÍNEZ-GLEZ, Victor et al. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas. Cancer Genetics and Cytogenetics, v. 196, n. 1, p. 1-6, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.08.003. Acesso em: 02 jul. 2025.
APA
Martínez-Glez, V., Alvarez, L., Franco-Hernández, C., Torres-Martin, M., Campos, J. M. de, Isla, A., et al. (2010). Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas. Cancer Genetics and Cytogenetics, 196( 1), 1-6. doi:10.1016/j.cancergencyto.2009.08.003
NLM
Martínez-Glez V, Alvarez L, Franco-Hernández C, Torres-Martin M, Campos JM de, Isla A, Vaquero J, Lassaletta L, Castresana JS, Casartelli C, Rey JA. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 1): 1-6.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
Vancouver
Martínez-Glez V, Alvarez L, Franco-Hernández C, Torres-Martin M, Campos JM de, Isla A, Vaquero J, Lassaletta L, Castresana JS, Casartelli C, Rey JA. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 1): 1-6.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
Artigo de periodico
Tetrasomy 8 in a patient with chronic lymphocytic leukemia (2010)
Oliveira, Fábio Morato de; Brandão, Renata Amorim; Cueva, Sabrina Dias Leite; Careta, Francisco de Paula; Simoes, Belinda Pinto; Rego, Eduardo Magalhaes; Falcao, Roberto Passetto
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: LEUCEMIA, CITOGENÉTICA
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ABNT
OLIVEIRA, Fábio Morato de et al. Tetrasomy 8 in a patient with chronic lymphocytic leukemia. Cancer Genetics and Cytogenetics, v. 198, n. 2, p. 166-169, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.12.016. Acesso em: 02 jul. 2025.
APA
Oliveira, F. M. de, Brandão, R. A., Cueva, S. D. L., Careta, F. de P., Simoes, B. P., Rego, E. M., & Falcao, R. P. (2010). Tetrasomy 8 in a patient with chronic lymphocytic leukemia. Cancer Genetics and Cytogenetics, 198( 2), 166-169. doi:10.1016/j.cancergencyto.2009.12.016
NLM
Oliveira FM de, Brandão RA, Cueva SDL, Careta F de P, Simoes BP, Rego EM, Falcao RP. Tetrasomy 8 in a patient with chronic lymphocytic leukemia [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 2): 166-169.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.12.016
Vancouver
Oliveira FM de, Brandão RA, Cueva SDL, Careta F de P, Simoes BP, Rego EM, Falcao RP. Tetrasomy 8 in a patient with chronic lymphocytic leukemia [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 2): 166-169.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.12.016
Artigo de periodico
Segmental amplification of MLL gene associated with high expression of AURKA and AURKB genes in a case of acute monoblastic leukemia with complex karyotype (2010)
Oliveira, Fábio Morato de; Araújo, Antonio Roberto Lucena de; Cueva, Sabrina Dias Leite; Santos, Guilherme Augusto Silva dos; Rego, Eduardo Magalhaes; Falcao, Roberto Passetto
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: LEUCEMIA, CITOGENÉTICA
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ABNT
OLIVEIRA, Fábio Morato de et al. Segmental amplification of MLL gene associated with high expression of AURKA and AURKB genes in a case of acute monoblastic leukemia with complex karyotype. Cancer Genetics and Cytogenetics, v. 198, n. 1, p. 62-65, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.12.005. Acesso em: 02 jul. 2025.
APA
Oliveira, F. M. de, Araújo, A. R. L. de, Cueva, S. D. L., Santos, G. A. S. dos, Rego, E. M., & Falcao, R. P. (2010). Segmental amplification of MLL gene associated with high expression of AURKA and AURKB genes in a case of acute monoblastic leukemia with complex karyotype. Cancer Genetics and Cytogenetics, 198( 1), 62-65. doi:10.1016/j.cancergencyto.2009.12.005
NLM
Oliveira FM de, Araújo ARL de, Cueva SDL, Santos GAS dos, Rego EM, Falcao RP. Segmental amplification of MLL gene associated with high expression of AURKA and AURKB genes in a case of acute monoblastic leukemia with complex karyotype [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 62-65.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.12.005
Vancouver
Oliveira FM de, Araújo ARL de, Cueva SDL, Santos GAS dos, Rego EM, Falcao RP. Segmental amplification of MLL gene associated with high expression of AURKA and AURKB genes in a case of acute monoblastic leukemia with complex karyotype [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 62-65.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.12.005
Artigo de periodico
Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity (2009)
Franco-Hernández, Carmen; Martínez-Glez, Victor; Campos, Jose M. de; Isla, Alberto; Vaquero, Jesús; Gutiérrez, Manuel; Casartelli, Cacilda; Rey, Juan A.
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: NEOPLASIAS, GENÉTICA
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ABNT
FRANCO-HERNÁNDEZ, Carmen et al. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity. Cancer Genetics and Cytogenetics, v. 190, n. 2, p. 93-96, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2008.09.017. Acesso em: 02 jul. 2025.
APA
Franco-Hernández, C., Martínez-Glez, V., Campos, J. M. de, Isla, A., Vaquero, J., Gutiérrez, M., et al. (2009). Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity. Cancer Genetics and Cytogenetics, 190( 2), 93-96. doi:10.1016/j.cancergencyto.2008.09.017
NLM
Franco-Hernández C, Martínez-Glez V, Campos JM de, Isla A, Vaquero J, Gutiérrez M, Casartelli C, Rey JA. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity [Internet]. Cancer Genetics and Cytogenetics. 2009 ; 190( 2): 93-96.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
Vancouver
Franco-Hernández C, Martínez-Glez V, Campos JM de, Isla A, Vaquero J, Gutiérrez M, Casartelli C, Rey JA. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity [Internet]. Cancer Genetics and Cytogenetics. 2009 ; 190( 2): 93-96.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
Artigo de periodico-carta/editorial
Insertion (15;14)(q22;q13q32) in a case of Ph+ ALL... [Carta] (2008)
Oliveira, Fábio Morato de; Falcão, Roberto Passetto; Pontes, Lorena Lobo de Figueiredo; Simões, Belinda Pinto; Tone, Luiz Gonzaga
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: LEUCEMIA, CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Fábio Morato de et al. Insertion (15;14)(q22;q13q32) in a case of Ph+ ALL.. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 02 jul. 2025. , 2008
APA
Oliveira, F. M. de, Falcão, R. P., Pontes, L. L. de F., Simões, B. P., & Tone, L. G. (2008). Insertion (15;14)(q22;q13q32) in a case of Ph+ ALL.. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Oliveira FM de, Falcão RP, Pontes LL de F, Simões BP, Tone LG. Insertion (15;14)(q22;q13q32) in a case of Ph+ ALL.. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185 65-67.[citado 2025 jul. 02 ]
Vancouver
Oliveira FM de, Falcão RP, Pontes LL de F, Simões BP, Tone LG. Insertion (15;14)(q22;q13q32) in a case of Ph+ ALL.. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185 65-67.[citado 2025 jul. 02 ]
Artigo de periodico-carta/editorial
Mutation analysis of the CITED4 gene in glioblastomas. [Carta] (2008)
Torres-Martín; Franco-Hernandez, Carmen; Matinez-Glez, Victor; Campos, Jose M. de; Isla, Alberto; Casartelli, Cacilda; Rey, Juan A.
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: POLIMORFISMO, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TORRES-MARTÍN, et al. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 02 jul. 2025. , 2008
APA
Torres-Martín,, Franco-Hernandez, C., Matinez-Glez, V., Campos, J. M. de, Isla, A., Casartelli, C., & Rey, J. A. (2008). Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Torres-Martín, Franco-Hernandez C, Matinez-Glez V, Campos JM de, Isla A, Casartelli C, Rey JA. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185( 2): 114-116.[citado 2025 jul. 02 ]
Vancouver
Torres-Martín, Franco-Hernandez C, Matinez-Glez V, Campos JM de, Isla A, Casartelli C, Rey JA. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185( 2): 114-116.[citado 2025 jul. 02 ]
Artigo de periodico
Acute myeloid leukemia (AML-M2) with t(5;11)(q35;q13) and normal expression of cyclin D1 (2007)
Oliveira, Fábio Morato de; Tone, Luiz Gonzaga; Simões, Belinda Pinto; Falcão, Roberto Passetto; Brassesco, Maria Sol; Sakamoto-Hojo, Elza Tiemi; Santos, Guilherme Augusto Silva dos; Marinato, André Fiorin; Jácomo, Rafael Henriques; Rego, Eduardo Magalhães
Fonte: Cancer Genetics and Cytogenetics. Unidades: FMRP, FFCLRP
Assuntos: LEUCEMIA, CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Fábio Morato de et al. Acute myeloid leukemia (AML-M2) with t(5;11)(q35;q13) and normal expression of cyclin D1. Cancer Genetics and Cytogenetics, v. 172, n. 2, p. 154-157, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2006.09.004. Acesso em: 02 jul. 2025.
APA
Oliveira, F. M. de, Tone, L. G., Simões, B. P., Falcão, R. P., Brassesco, M. S., Sakamoto-Hojo, E. T., et al. (2007). Acute myeloid leukemia (AML-M2) with t(5;11)(q35;q13) and normal expression of cyclin D1. Cancer Genetics and Cytogenetics, 172( 2), 154-157. doi:10.1016/j.cancergencyto.2006.09.004
NLM
Oliveira FM de, Tone LG, Simões BP, Falcão RP, Brassesco MS, Sakamoto-Hojo ET, Santos GAS dos, Marinato AF, Jácomo RH, Rego EM. Acute myeloid leukemia (AML-M2) with t(5;11)(q35;q13) and normal expression of cyclin D1 [Internet]. Cancer Genetics and Cytogenetics. 2007 ; 172( 2): 154-157.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2006.09.004
Vancouver
Oliveira FM de, Tone LG, Simões BP, Falcão RP, Brassesco MS, Sakamoto-Hojo ET, Santos GAS dos, Marinato AF, Jácomo RH, Rego EM. Acute myeloid leukemia (AML-M2) with t(5;11)(q35;q13) and normal expression of cyclin D1 [Internet]. Cancer Genetics and Cytogenetics. 2007 ; 172( 2): 154-157.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2006.09.004
Artigo de periodico-carta/editorial
Acute lymphoblastic leukemia with inv(5)(q13q31) in a pediatric patient. [Carta] (2006)
Oliveira, Fábio Morato de; Scrideli, Carlos Alberto; Queiroz, Rosane Gomes de Paula; Tone, Luiz Gonzaga
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: LEUCEMIA, PEDIATRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Fábio Morato de et al. Acute lymphoblastic leukemia with inv(5)(q13q31) in a pediatric patient. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 02 jul. 2025. , 2006
APA
Oliveira, F. M. de, Scrideli, C. A., Queiroz, R. G. de P., & Tone, L. G. (2006). Acute lymphoblastic leukemia with inv(5)(q13q31) in a pediatric patient. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Oliveira FM de, Scrideli CA, Queiroz RG de P, Tone LG. Acute lymphoblastic leukemia with inv(5)(q13q31) in a pediatric patient. [Carta]. Cancer Genetics and Cytogenetics. 2006 ; 165 81-82.[citado 2025 jul. 02 ]
Vancouver
Oliveira FM de, Scrideli CA, Queiroz RG de P, Tone LG. Acute lymphoblastic leukemia with inv(5)(q13q31) in a pediatric patient. [Carta]. Cancer Genetics and Cytogenetics. 2006 ; 165 81-82.[citado 2025 jul. 02 ]
Artigo de periodico
Differentially expressed genes in the prostate cancer cell line LNCaP after exposure to androgen and anti-androgen (2006)
Coutinho-Camillo, Cláudia M.; Salaorni, Sibeli; Sarkis, Álvaro S.; Nagai, Maria A.
Fonte: Cancer Genetics and Cytogenetics. Unidade: FM
Assuntos: ANDRÓGENOS, GENES, NEOPLASIAS, NEOPLASIAS PROSTÁTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COUTINHO-CAMILLO, Cláudia M. et al. Differentially expressed genes in the prostate cancer cell line LNCaP after exposure to androgen and anti-androgen. Cancer Genetics and Cytogenetics, v. 166, p. 130-138, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2005.09.012. Acesso em: 02 jul. 2025.
APA
Coutinho-Camillo, C. M., Salaorni, S., Sarkis, Á. S., & Nagai, M. A. (2006). Differentially expressed genes in the prostate cancer cell line LNCaP after exposure to androgen and anti-androgen. Cancer Genetics and Cytogenetics, 166, 130-138. doi:10.1016/j.cancergencyto.2005.09.012
NLM
Coutinho-Camillo CM, Salaorni S, Sarkis ÁS, Nagai MA. Differentially expressed genes in the prostate cancer cell line LNCaP after exposure to androgen and anti-androgen [Internet]. Cancer Genetics and Cytogenetics. 2006 ; 166 130-138.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2005.09.012
Vancouver
Coutinho-Camillo CM, Salaorni S, Sarkis ÁS, Nagai MA. Differentially expressed genes in the prostate cancer cell line LNCaP after exposure to androgen and anti-androgen [Internet]. Cancer Genetics and Cytogenetics. 2006 ; 166 130-138.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2005.09.012
Artigo de periodico
An intronic variant in the TP53 gene in a Brazilian woman with breast cancer (2005)
Lacerda, Leandra Linhares; Serrano, Sérgio Vicente; Mathes, Ângelo do Carmo da Silva; Rey, Juan A.; Bello, Maria Josefa; Casartelli, Cacilda
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: NEOPLASIAS MAMÁRIAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LACERDA, Leandra Linhares et al. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer. Cancer Genetics and Cytogenetics, v. 160, p. 160-163, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2004.11.014. Acesso em: 02 jul. 2025.
APA
Lacerda, L. L., Serrano, S. V., Mathes, Â. do C. da S., Rey, J. A., Bello, M. J., & Casartelli, C. (2005). An intronic variant in the TP53 gene in a Brazilian woman with breast cancer. Cancer Genetics and Cytogenetics, 160, 160-163. doi:10.1016/j.cancergencyto.2004.11.014
NLM
Lacerda LL, Serrano SV, Mathes Â do C da S, Rey JA, Bello MJ, Casartelli C. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer [Internet]. Cancer Genetics and Cytogenetics. 2005 ; 160 160-163.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
Vancouver
Lacerda LL, Serrano SV, Mathes Â do C da S, Rey JA, Bello MJ, Casartelli C. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer [Internet]. Cancer Genetics and Cytogenetics. 2005 ; 160 160-163.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
Artigo de periodico
Detection of micronuclei formation and nuclear anomalies in regenerative nodules of human cirrhotic livers and relationship to hepatocellular carcinoma (2004)
Almeida, Terezinha M. B. de; Leitao, Regina C.; Andrade, Joyce D.; Becak, Willy; Carrilho, Flair Jose; Sonohara, Shigueko
Fonte: Cancer Genetics and Cytogenetics. Unidade: FM
Assuntos: CIRROSE HEPÁTICA (PATOLOGIA), NEOPLASIAS HEPÁTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA, Terezinha M. B. de et al. Detection of micronuclei formation and nuclear anomalies in regenerative nodules of human cirrhotic livers and relationship to hepatocellular carcinoma. Cancer Genetics and Cytogenetics, v. 150, p. 16-21, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2003.08.001. Acesso em: 02 jul. 2025.
APA
Almeida, T. M. B. de, Leitao, R. C., Andrade, J. D., Becak, W., Carrilho, F. J., & Sonohara, S. (2004). Detection of micronuclei formation and nuclear anomalies in regenerative nodules of human cirrhotic livers and relationship to hepatocellular carcinoma. Cancer Genetics and Cytogenetics, 150, 16-21. doi:10.1016/j.cancergencyto.2003.08.001
NLM
Almeida TMB de, Leitao RC, Andrade JD, Becak W, Carrilho FJ, Sonohara S. Detection of micronuclei formation and nuclear anomalies in regenerative nodules of human cirrhotic livers and relationship to hepatocellular carcinoma [Internet]. Cancer Genetics and Cytogenetics. 2004 ; 150 16-21.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2003.08.001
Vancouver
Almeida TMB de, Leitao RC, Andrade JD, Becak W, Carrilho FJ, Sonohara S. Detection of micronuclei formation and nuclear anomalies in regenerative nodules of human cirrhotic livers and relationship to hepatocellular carcinoma [Internet]. Cancer Genetics and Cytogenetics. 2004 ; 150 16-21.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/j.cancergencyto.2003.08.001
Artigo de periodico
Fusion of CO1A1 exon 29 with PDGFB exon 2 in a der (22)t(17;22) in a pediatric giant cell fibroblastoma with a pigmented Bednar tumor component: evidence for age-related chromosomal pattern in dermatofibrosarcoma protuberans and related tumors (2002)
Maire, Georges; Martin, Ludovic; Provost, Sophie Michalak; Gattás, Gilka Jorge Figaro; Carel, Claude Turc; Lorette, Gérard; Pedeutour, Florence
Fonte: Cancer Genetics and Cytogenetics. Unidade: FM
Assuntos: GENÉTICA, CITOGENÉTICA, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAIRE, Georges et al. Fusion of CO1A1 exon 29 with PDGFB exon 2 in a der (22)t(17;22) in a pediatric giant cell fibroblastoma with a pigmented Bednar tumor component: evidence for age-related chromosomal pattern in dermatofibrosarcoma protuberans and related tumors. Cancer Genetics and Cytogenetics, v. 134, p. 156-161, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00617-3. Acesso em: 02 jul. 2025.
APA
Maire, G., Martin, L., Provost, S. M., Gattás, G. J. F., Carel, C. T., Lorette, G., & Pedeutour, F. (2002). Fusion of CO1A1 exon 29 with PDGFB exon 2 in a der (22)t(17;22) in a pediatric giant cell fibroblastoma with a pigmented Bednar tumor component: evidence for age-related chromosomal pattern in dermatofibrosarcoma protuberans and related tumors. Cancer Genetics and Cytogenetics, 134, 156-161. doi:10.1016/s0165-4608(01)00617-3
NLM
Maire G, Martin L, Provost SM, Gattás GJF, Carel CT, Lorette G, Pedeutour F. Fusion of CO1A1 exon 29 with PDGFB exon 2 in a der (22)t(17;22) in a pediatric giant cell fibroblastoma with a pigmented Bednar tumor component: evidence for age-related chromosomal pattern in dermatofibrosarcoma protuberans and related tumors [Internet]. Cancer Genetics and Cytogenetics. 2002 ; 134 156-161.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(01)00617-3
Vancouver
Maire G, Martin L, Provost SM, Gattás GJF, Carel CT, Lorette G, Pedeutour F. Fusion of CO1A1 exon 29 with PDGFB exon 2 in a der (22)t(17;22) in a pediatric giant cell fibroblastoma with a pigmented Bednar tumor component: evidence for age-related chromosomal pattern in dermatofibrosarcoma protuberans and related tumors [Internet]. Cancer Genetics and Cytogenetics. 2002 ; 134 156-161.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(01)00617-3
Artigo de periodico
Analysis of p73 gene in meningiomas with deletion at 1p (2001)
Lomas, Jesus; Bello, Josefa; Arjona, Dolores; Gonzales-Gomez, Pilar; Alonso, M. Eva; Campos, José M. de; Vaquero, Jesus; Ruiz-Barnes, Pedro; Sarasa, José L.; Casartelli, Cacilda; Rey, Juan A.
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assunto: MENINGIOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOMAS, Jesus et al. Analysis of p73 gene in meningiomas with deletion at 1p. Cancer Genetics and Cytogenetics, v. 129, p. 88-91, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00430-7. Acesso em: 02 jul. 2025.
APA
Lomas, J., Bello, J., Arjona, D., Gonzales-Gomez, P., Alonso, M. E., Campos, J. M. de, et al. (2001). Analysis of p73 gene in meningiomas with deletion at 1p. Cancer Genetics and Cytogenetics, 129, 88-91. doi:10.1016/s0165-4608(01)00430-7
NLM
Lomas J, Bello J, Arjona D, Gonzales-Gomez P, Alonso ME, Campos JM de, Vaquero J, Ruiz-Barnes P, Sarasa JL, Casartelli C, Rey JA. Analysis of p73 gene in meningiomas with deletion at 1p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 88-91.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7
Vancouver
Lomas J, Bello J, Arjona D, Gonzales-Gomez P, Alonso ME, Campos JM de, Vaquero J, Ruiz-Barnes P, Sarasa JL, Casartelli C, Rey JA. Analysis of p73 gene in meningiomas with deletion at 1p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 88-91.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7
Artigo de periodico
Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma (2001)
Espinoza, Luis A.; Barbieri Neto, José; Popescu, Nicholas C.; Casartelli, Cacilda
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: LINFOMA, TESTÍCULO, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESPINOZA, Luis A. et al. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma. Cancer Genetics and Cytogenetics, v. 131, p. 79-81, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00495-2. Acesso em: 02 jul. 2025.
APA
Espinoza, L. A., Barbieri Neto, J., Popescu, N. C., & Casartelli, C. (2001). Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma. Cancer Genetics and Cytogenetics, 131, 79-81. doi:10.1016/s0165-4608(01)00495-2
NLM
Espinoza LA, Barbieri Neto J, Popescu NC, Casartelli C. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 131 79-81.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(01)00495-2
Vancouver
Espinoza LA, Barbieri Neto J, Popescu NC, Casartelli C. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 131 79-81.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(01)00495-2
Artigo de periodico
Aneurysmal bone cyst with chromosomal changes involving 7q and 16p (2001)
Baruffi, Marcelo Razera; Barbieri Neto, José; Barbieri, Claudio Henrique; Casartelli, Cacilda
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: CISTOS, OSSO E OSSOS, CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARUFFI, Marcelo Razera et al. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p. Cancer Genetics and Cytogenetics, v. 129, p. 177-180, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00453-8. Acesso em: 02 jul. 2025.
APA
Baruffi, M. R., Barbieri Neto, J., Barbieri, C. H., & Casartelli, C. (2001). Aneurysmal bone cyst with chromosomal changes involving 7q and 16p. Cancer Genetics and Cytogenetics, 129, 177-180. doi:10.1016/s0165-4608(01)00453-8
NLM
Baruffi MR, Barbieri Neto J, Barbieri CH, Casartelli C. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 177-180.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(01)00453-8
Vancouver
Baruffi MR, Barbieri Neto J, Barbieri CH, Casartelli C. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 177-180.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(01)00453-8
Artigo de periodico
Osteoid osteomas with chromosome alterations involving 22q (2001)
Baruffi, Marcelo Razera; Volpon, José Batista; Barbieri Neto, José; Casartelli, Cacilda
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: ONCOLOGIA, OSSO E OSSOS (CIRURGIA), CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARUFFI, Marcelo Razera et al. Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, v. 124, p. 127-131, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(00)00327-7. Acesso em: 02 jul. 2025.
APA
Baruffi, M. R., Volpon, J. B., Barbieri Neto, J., & Casartelli, C. (2001). Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, 124, 127-131. doi:10.1016/s0165-4608(00)00327-7
NLM
Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
Vancouver
Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2025 jul. 02 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
Artigo de periodico
Pathological and karyotypic abnormalities in advanced gastric carcinomas (1999)
Espinoza, Luis A; Barbieri Neto, José; Casartelli, Cacilda
Fonte: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assuntos: ONCOLOGIA, GENÉTICA MÉDICA, GASTROENTEROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESPINOZA, Luis A e BARBIERI NETO, José e CASARTELLI, Cacilda. Pathological and karyotypic abnormalities in advanced gastric carcinomas. Cancer Genetics and Cytogenetics, v. 109, n. 1, p. 45-50, 1999Tradução . . Acesso em: 02 jul. 2025.
APA
Espinoza, L. A., Barbieri Neto, J., & Casartelli, C. (1999). Pathological and karyotypic abnormalities in advanced gastric carcinomas. Cancer Genetics and Cytogenetics, 109( 1), 45-50.
NLM
Espinoza LA, Barbieri Neto J, Casartelli C. Pathological and karyotypic abnormalities in advanced gastric carcinomas. Cancer Genetics and Cytogenetics. 1999 ; 109( 1): 45-50.[citado 2025 jul. 02 ]
Vancouver
Espinoza LA, Barbieri Neto J, Casartelli C. Pathological and karyotypic abnormalities in advanced gastric carcinomas. Cancer Genetics and Cytogenetics. 1999 ; 109( 1): 45-50.[citado 2025 jul. 02 ]

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